9 results for author:"Coumel P." in Literature citations
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| Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Schwartz P.J., Priori S.G., Spazzolini C., Moss A.J., Vincent G.M., Napolitano C., Denjoy I., Guicheney P., Breithardt G., Keating M.T. et al. Circulation 103:89-95(2001) · Mapped (28) |
| Congenital long QT syndrome. The value of genetics in prognostic evaluation. Denjoy I., Lupoglazoff J.M., Donger C., Berthet M., Richard P., Neyroud N., Villain E., Lucet V., Coumel P., Guicheney P. Arch. Mal. Coeur Vaiss. 92:557-563(1999) · UniProtKB (1) |
| C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence. Berthet M., Denjoy I., Donger C., Demay L., Hammoude H., Klug D., Schulze-Bahr E., Richard P., Funke H., Schwartz K. et al. Circulation 99:1464-1470(1999) · UniProtKB (1) |
| Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome. Neyroud N., Richard P., Vignier N., Donger C., Denjoy I., Demay L., Shkolnikova M., Pesce R., Chevalier P., Hainque B. et al. Circ. Res. 84:290-297(1999) · UniProtKB (1) |
| Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome. Neyroud N., Denjoy I., Donger C., Gary F., Villain E., Leenhardt A., Benali K., Schwartz K., Coumel P., Guicheney P. Eur. J. Hum. Genet. 6:129-133(1998) · UniProtKB (1) |
| KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome. Donger C., Denjoy I., Berthet M., Neyroud N., Cruaud C., Bennaceur M., Chivoret G., Schwartz K., Coumel P., Guicheney P. Circulation 96:2778-2781(1997) · UniProtKB (1) |
| A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Neyroud N., Tesson F., Denjoy I., Leibovici M., Donger C., Barhanin J., Faure S., Gary F., Coumel P., Petit C. et al. Nat. Genet. 15:186-189(1997) |
| Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome. Tesson F., Donger C., Denjoy I., Berthet M., Bennaceur M., Petit C., Coumel P., Schwartz K., Guicheney P. J. Mol. Cell. Cardiol. 28:2051-2055(1996) · UniProtKB (1) |
| A mutation in HERG associated with notched T waves in long QT syndrome. Dausse E., Berthet M., Denjoy I., Andre-Fouet X., Cruaud C., Bennaceur M., Faure S., Coumel P., Schwartz K., Guicheney P. J. Mol. Cell. Cardiol. 28:1609-1615(1996) · UniProtKB (1) |